ClinVar Miner

Submissions for variant NM_031942.5(CDCA7):c.895-5T>C

gnomAD frequency: 0.00009  dbSNP: rs2288992
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002121153 SCV002445605 benign not provided 2024-01-08 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003923740 SCV004737874 likely benign CDCA7-related disorder 2019-09-13 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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